Division of Anatomic Pathology, Mayo Clinic, Rochester, MN 55905, USA.
Division of Anatomic Pathology, Mayo Clinic, Rochester, MN 55905, USA.
Semin Diagn Pathol. 2019 Nov;36(6):423-433. doi: 10.1053/j.semdp.2019.07.007. Epub 2019 Jul 24.
Immunoglobuline G4-related disease (IgG4-RD) is a systemic disease that can involve virtually any organs including the biliary tract and liver. The biliary tract involvement of IgG4-RD is known as IgG4-sclerosing cholangitis (IgG4-SC) and may or may not present with an inflammatory pseudotumor. Large bile ducts such as extrahepatic, hilar, and perihilar ducts are typically affected and demonstrate marked bile duct wall thickening and develop strictures. Histologically, the involved ducts show transmural dense lymphoplasmacytic infiltrates with storiform fibrosis extending into peribiliary glands and periductal soft tissue. The luminal epithelium is usually preserved. Tissue eosinophilia and obliterative phlebitis are also frequently noted. Liver biopsy findings of IgG4-SC are heterogeneous and rather nonspecific, but two features specific to IgG4-SC have been described: >10 IgG4-positive plasma cell/HPF and small portal-based fibroinflammatory nodules. Secondary changes, due to downstream bile duct obstruction are often appreciated. When considering the differential diagnosis, primary sclerosing cholangitis and cholangiocarcinoma are great clinical and histologic mimics of IgG4-SC. Liver involvement in IgG4-RD has not been well characterized and includes IgG4-hepatopathy and IgG4-related autoimmune hepatitis (AIH). IgG4-hepatopathy is a generic term covering hepatic lesions related to IgG4-RD and /or IgG4-SC. It includes primary liver parenchymal changes inherent to IgG4-RD, liver parenchymal involvement of IgG4-SC, and secondary changes related to IgG4-SC. IgG4-related AIH is characterized by clinical and histologic features of classical AIH but with prominent (>10/HPF) IgG4-positive plasma cells. It is unclear whether this represents a hepatic manifestation of IgG4-RD or a subset of AIH with increased IgG4-positive plasma cells at the present time. Synchronous or metachronous involvement of other organs, offers a clue to make this distinction. IgG4 immunohistochemistry has an important role in diagnosing IgG4-RD. But the diagnosis cannot be made solely based on the number of IgG4-positive plasma cells, and results need to be interpreted with caution as increased IgG4-positive plasma cells can be seen in other inflammatory conditions or even in malignancy.
免疫球蛋白 G4 相关疾病(IgG4-RD)是一种可累及包括胆道和肝脏在内的几乎所有器官的系统性疾病。IgG4-RD 的胆道受累称为 IgG4 硬化性胆管炎(IgG4-SC),可能伴有或不伴有炎症性假瘤。大胆管如肝外、肝门和肝周胆管通常受累,表现为明显的胆管壁增厚和狭窄。组织学上,受累胆管表现为壁内致密的淋巴浆细胞浸润,伴有向胆管周围腺体和胆管周围软组织延伸的纤维组织增生。管腔上皮通常保留。组织嗜酸性粒细胞浸润和闭塞性静脉炎也经常被发现。IgG4-SC 的肝活检表现为异质性且非特异性,但已描述了两种与 IgG4-SC 相关的特征性表现:每高倍镜视野(HPF)>10 个 IgG4 阳性浆细胞和小的门管区纤维炎症性小结节。由于下游胆管阻塞引起的继发性改变通常也很明显。在考虑鉴别诊断时,原发性硬化性胆管炎和胆管癌是 IgG4-SC 的重要临床和组织学模拟物。IgG4-RD 的肝脏受累尚未得到很好的描述,包括 IgG4 肝炎和 IgG4 相关自身免疫性肝炎(AIH)。IgG4 肝炎是一个涵盖与 IgG4-RD 和/或 IgG4-SC 相关的肝病变的通用术语。它包括 IgG4-RD 固有肝脏实质改变、IgG4-SC 的肝实质受累以及与 IgG4-SC 相关的继发性改变。IgG4 相关 AIH 的特征是具有典型 AIH 的临床和组织学特征,但 IgG4 阳性浆细胞明显增多(>10/HPF)。目前尚不清楚这是 IgG4-RD 的肝脏表现还是 AIH 的一个子集,其 IgG4 阳性浆细胞增多。其他器官的同步或异时性受累为做出这种区分提供了线索。IgG4 免疫组化在诊断 IgG4-RD 中具有重要作用。但是,不能仅根据 IgG4 阳性浆细胞的数量来做出诊断,并且需要谨慎解释结果,因为在其他炎症性疾病甚至恶性肿瘤中也可以看到 IgG4 阳性浆细胞增多。